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1,1'-Carbonyldiimidazole → 1-Phenyl-5-phenoxy-3,4-dihydro-(1H)-quinazolin-2-one

HRID 1826835
ノート
印刷プレビュー

反応式

HRID 1826835 の反応式
[O:1]([C:8]1[CH:15]=[CH:14][CH:13]=[C:12]([NH:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:9]=1[CH2:10][NH2:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:23](N1C=CN=C1)(N1C=CN=C1)=[O:24]>O1CCCC1>[C:17]1([N:16]2[C:12]3[C:9](=[C:8]([O:1][C:2]4[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=4)[CH:15]=[CH:14][CH:13]=3)[CH2:10][NH:11][C:23]2=[O:24])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 682631,1'-CarbonyldiimidazoleHCID 221362242-Phenoxy-6-(phenylamino)benzylamine

生成物 1

HCID 98617161-Phenyl-5-phenoxy-3,4-dihydro-(1H)-quinazolin-2-one

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

The product of example 1c above, 2-phenoxy-6-(phenylamino)benzyl amine, (0.165 g 0.57 mmol) was dissolved in dry tetrahydrofuran (5 mL) and stirred under argon at room temperature. 1,1′-Carbonyldiimidazole (0.120 g, 0.74 mmol) dissolved in dry tetrahydrofuran (2 mL) was added and the mixture stirred at room temperature. The solvent was evaporated in vacuo, to give the crude product which was flash chromatographed on silica gel eluted with 0–2% methanol in methylene chloride to give to the title compound as a white amorphous solid. mp 225–227° C.

後処理

  1. additionwas added
  2. stirringthe mixture stirred at room temperature
  3. customThe solvent was evaporated in vacuo
  4. customto give the crude product which
  5. customchromatographed on silica gel
  6. washeluted with 0–2% methanol in methylene chloride

出典と根拠

ORDレコード
ord-f69158d16e4d45d1aab76335f5715877
出典データセット
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07053099B1

反応ノート

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